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利用肾类器官进行疾病建模。

Disease Modeling with Kidney Organoids.

作者信息

Karp Sophie, Pollak Martin R, Subramanian Balajikarthick

机构信息

Division of Nephrology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

出版信息

Micromachines (Basel). 2022 Aug 25;13(9):1384. doi: 10.3390/mi13091384.

Abstract

Kidney diseases often lack optimal treatments, causing millions of deaths each year. Thus, developing appropriate model systems to study human kidney disease is of utmost importance. Some of the most promising human kidney models are organoids or small organ-resembling tissue collectives, derived from human-induced pluripotent stem cells (hiPSCs). However, they are more akin to a first-trimester fetal kidney than an adult kidney. Therefore, new strategies are needed to advance their maturity. They have great potential for disease modeling and eventually auxiliary therapy if they can reach the maturity of an adult kidney. In this review, we will discuss the current state of kidney organoids in terms of their similarity to the human kidney and use as a disease modeling system thus far. We will then discuss potential pathways to advance the maturity of kidney organoids to match an adult kidney for more accurate human disease modeling.

摘要

肾脏疾病往往缺乏理想的治疗方法,每年导致数百万人死亡。因此,开发合适的模型系统来研究人类肾脏疾病至关重要。一些最有前景的人类肾脏模型是类器官或类似小器官的组织聚集体,它们由人类诱导多能干细胞(hiPSCs)衍生而来。然而,它们更类似于孕早期的胎儿肾脏,而非成人肾脏。因此,需要新的策略来促进它们的成熟。如果它们能够达到成人肾脏的成熟度,那么在疾病建模以及最终的辅助治疗方面将具有巨大潜力。在这篇综述中,我们将讨论肾脏类器官目前与人类肾脏的相似程度以及迄今为止作为疾病建模系统的应用情况。然后,我们将讨论促进肾脏类器官成熟以匹配成人肾脏从而实现更精确人类疾病建模的潜在途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05a0/9506184/cebd9c709cbc/micromachines-13-01384-g001.jpg

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